Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
  • C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
  • C08G81/024—Block or graft polymers containing sequences of polymers of C08C or C08F and of polymers of C08G
  • C08G81/025—Block or graft polymers containing sequences of polymers of C08C or C08F and of polymers of C08G containing polyether sequences
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
  • C08F214/18—Monomers containing fluorine
  • C08F214/22—Vinylidene fluoride
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
  • B01D67/0002—Organic membrane manufacture
  • B01D67/0023—Organic membrane manufacture by inducing porosity into non porous precursor membranes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
  • C08F214/18—Monomers containing fluorine
  • C08F214/22—Vinylidene fluoride
  • C08F214/225—Vinylidene fluoride with non-fluorinated comonomers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
  • C08G65/002—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds
  • C08G65/005—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens
  • C08G65/007—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens containing fluorine
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
  • C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
  • C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
  • C08L27/16—Homopolymers or copolymers or vinylidene fluoride
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
  • C08G2261/10—Definition of the polymer structure
  • C08G2261/12—Copolymers
  • C08G2261/128—Copolymers graft
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
  • C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
  • C08G2650/46—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing halogen
  • C08G2650/48—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing halogen containing fluorine, e.g. perfluropolyethers
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L2205/00—Polymer mixtures characterised by other features
  • C08L2205/05—Polymer mixtures characterised by other features containing polymer components which can react with one another

Definitions

• the present invention pertains to grafted fluoropolymers, to a process for their manufacture and to uses of said grafted fluoropolymers for manufacturing porous membranes.
• PVDF Polyvinylidene fluoride
• Biofouling is largely attributable to accumulated extracellular materials, rather than individual bacterial cells or microbial flocs.
• extracellular materials including soluble microbial products and extracellular polymeric substances, consist mainly of polysaccharides, proteins and natural organic matter.
• hydrophilic microfiltration and ultrafiltration membranes prepared from chemically or physically modified PVDF have been widely studied and reported.
• Several approaches have been developed to endow the membranes with hydrophylic properties, such as surface coating and surface grafting.
• WO 2012/175416 (SOLVAY SPECIALTY POLYMERS ITALY S.P.A.) Dec. 27, 2012 discloses a process for the manufacture of porous membranes, said process comprising providing a composition comprising at least one fluoropolymer, said fluoropolymer comprising recurring units derived from at least one (meth)acrylic monomer, and at least one poly(alkylene oxide).
• the poly(alkylene oxide) has a number average molecular weight typically comprised between 100000 and 5000000.
• US 2007/0219322 (MASSACHUSETTS INSTITUTE OF TECHNOLOGY) Sep. 20, 2007 discloses a process for the manufacture of graft copolymers via a controlled free-radical process by grafting hydrophilic chains onto polymers, particularly hydrophobic polymers such as polyvinyl chloride), PVDF and chlorinated polypropylene.
• the hydrophilic chain can comprise a poly(ethylene oxide).
• Membranes for water filtration can be prepared from the graft copolymers thereby provided.
• coating or surface grafting directly on a membrane has some shortcomings.
• a coated surface layer that is physically absorbed on the membrane's surface can be easily washed off and surface grafting of membranes is likely to be accompanied by changes in membrane pore size and distribution, which results in reduced permeability.
• composition (F) comprising at least one grafted fluoropolymer [polymer (Fg)] obtainable by the process of the invention, said polymer (Fg) comprising:
• the Applicant has surprisingly found that the grafted fluoropolymer of the present invention is endowed with outstanding hydrophilic properties to be suitably used for manufacturing porous membranes such as antifouling membranes for water purification.
• composition (F) of the invention typically comprises:
• fluoropolymer it is hereby intended to denote a polymer comprising recurring units derived from at least one fluorinated monomer.
• fluorinated monomer it is hereby intended to denote an ethylenically unsaturated monomer comprising at least one fluorine atom.
• the polymer (F) typically comprises recurring units derived from at least one fluorinated monomer and from at least one hydrogenated monomer comprising at least one functional group selected from the group consisting of a hydroxyl group and a carboxylic acid group [monomer (H)].
• hydrophilic monomer it is hereby intended to denote an ethylenically unsaturated monomer comprising at least one hydrogen atom and free from fluorine atoms.
• fluorinated monomer is understood to mean that the polymer (F) may comprise recurring units derived from one or more than one fluorinated monomers.
• fluorinated monomers is understood, for the purposes of the present invention, both in the plural and the singular, that is to say that they denote both one or more than one fluorinated monomers as defined above.
• the term “at least one monomer (H)” is understood to mean that the polymer (F) may comprise recurring units derived from one or more than one monomers (H) as defined above.
• the expression “monomer (H)” is understood, for the purposes of the present invention, both in the plural and the singular, that is to say that they denote both one or more than one monomers (H) as defined above.
• the polymer (F) typically comprises at least one fluorinated backbone and at least one functional group selected from the group consisting of a hydroxyl group and a carboxylic acid group.
• the polymer (F) comprises preferably at least 0.01% by moles, more preferably at least 0.05% by moles, even more preferably at least 0.1% by moles of recurring units derived from at least one monomer (H) as defined above.
• the polymer (F) comprises preferably at most 20% by moles, more preferably at most 15% by moles, even more preferably at most 10% by moles, most preferably at most 3% by moles of recurring units derived from at least one monomer (H) as defined above.
• Determination of the average mole percentage of monomer (H) recurring units in polymer (F) can be performed by any suitable method. Mention can be notably made of acid-base titration methods, well suited e.g. for the determination of the acrylic acid content, of NMR methods, adequate for the quantification of monomers (H) comprising aliphatic hydrogen atoms in side chains, of weight balance based on total fed monomer (H) and unreacted residual monomer (H) during polymer (F) manufacture.
• the monomer (H) is preferably a (meth)acrylic monomer [monomer (MA)] of formula (II):
• polymer (F) comprise recurring units derived from at least one fluorinated monomer and from at least one (meth)acrylic monomer [monomer (MA)] of formula (II) as defined above, said polymer (F) typically comprises at least one fluorinated backbone and at least one functional group of formula —C(O)—O—R x , wherein R x is a hydrogen atom or a C 1 -C 5 hydrocarbon group comprising at least one hydroxyl group.
• the monomer (MA) preferably complies with formula (II-A) here below:
• Non-limitative examples of suitable monomers (MA) include, notably, acrylic acid, methacrylic acid, hydroxyethyl(meth)acrylate, hydroxypropyl(meth)acrylate, hydroxyethylhexyl(meth)acrylate.
• the monomer (MA) is even more preferably selected from the followings:
• the monomer (MA) is even more preferably acrylic acid (AA) or hydroxyethyl acrylate (HEA).
• Non limitative examples of suitable fluorinated monomers include, notably, the followings:
• the polymer (F) is preferably selected from the group consisting of:
• the polymer (F 1 ) preferably comprises:
• the polymer (F 1 ) can be manufactured by aqueous suspension polymerization or by aqueous emulsion polymerization processes.
• the polymer (F 1 ) is preferably manufactured by an aqueous suspension polymerization process as described in WO 2008/129041 (SOLVAY SOLEXIS S.P.A.) Oct. 30, 2008.
• the polymer (F 2 ) typically has a molar ratio between hydrogenated monomer(s) and fluorinated monomer(s) ranging from 30:70 to 70:30.
• the hydrogenated monomer is preferably ethylene, optionally in combination with other hydrogenated monomers.
• the polymer (F 2 ) preferably comprises:
• Polymers (F 2 ) wherein the fluorinated monomer is chlorotrifluoroethylene (CTFE) and the hydrogenated monomer is ethylene (E) will be identified herein below as ECTFE copolymers; polymers (F 2 ) wherein the fluorinated monomer is tetrafluoroethylene (TFE) and the hydrogenated monomer is ethylene (E) will be identified herein below as ETFE copolymers.
• ECTFE polymers are preferred.
• the polymer (F 2 ) can be manufactured by aqueous suspension polymerization or by aqueous emulsion polymerization processes.
• the polymer (F) is more preferably selected from polymers (F 1 ).
• the polyoxyalkylene (POA) of formula (I) as defined above is typically free from fluorine atoms.
• polyoxyalkylene (POA) of formula (I) as defined above is typically selected from the group consisting of:
• the polyoxyalkylene (POA) of formula (I) as defined above is preferably a polyoxyethylene (POE) complying with formula (I′): R B —(CH 2 —O) x —(CH 2 CH 2 O) n —(CH 2 —O) x′ —R C (I′) wherein at least one of R B and R C is a reactive group comprising at least one heteroatom selected from oxygen and nitrogen different from the hydroxyl group, the remaining, if any, being a —[O] z —CH 3 alkyl group, wherein z is 0 or 1, x and x′, equal to or different from each other, are independently 0 or 1, and n is an integer comprised between 2 and 1000, preferably between 5 and 200.
• the selection of the reactive group of the polyoxyalkylene (POA) of formula (I) as defined above is not particularly limited, provided that it is different from the hydroxyl group and it enables, under appropriate conditions, polycondensation and/or addition of the POA of formula (I) as defined above with the polymer (F) as defined above through one or more functional groups.
• the reactive group of the POA of formula (I) as defined above typically enables polycondensation and/or addition of the POA of formula (I) as defined above with the polymer (F) as defined above through one or more functional groups selected from the group consisting of an ester group, an ether group and an urethane group.
• the reactive group of the POA of formula (I) as defined above preferably comprises at least one functional group selected from a sulfonic ester group of formula —[O] z —SO 2 R, wherein R is a C 1 -C 8 fluorinated or hydrogenated group optionally comprising one or more aromatic rings and z is 0 or 1, a carboxylic acid group, an epoxide functional group and an isocyanate functional group.
• the reactive group of the POA of formula (I) as defined above is preferably selected from the group consisting of:
• the divalent hydrocarbon group E may be selected from the followings:
• Non-limitative examples of suitable divalent hydrocarbon groups E include, notably, those derived from poly(ethylene adipate)-tolylene 2,4-diisocyanate, poly(propylene glycol)-tolylene 2,4-diisocyanate, hexamethylendiisocyanate, trimethylhexamethylenediisocyanate, isophoron diisocyanate, 4,4′-methylenebis(cyclohexylisocyanate), cyclohexyl-1,4-diisocyanate, 4,4′-methylenebis(phenylisocyanate) or its isomers, toluene 2,4-diisocyanate or isomers thereof, xylylene diisocyanate, naphthalene-1,5-diisocyanate, p-phenylen-diisocyanate.
• Non-limitative examples of suitable polyoxyethylenes (POEs) of formula (I-A) include, notably, the followings:
• fluorinated backbone it is hereby intended to denote a fluoropolymer chain comprising recurring units derived from one or more fluorinated monomers and from one or more hydrogenated monomers, said recurring units being randomly distributed along the backbone chain.
• the fluorinated backbone of the polymer (Fg) is preferably selected from the group consisting of:
• the polymer (F) in the process of the invention comprise recurring units derived from at least one fluorinated monomer and from at least one (meth)acrylic monomer [monomer (MA)] of formula (II) as defined above
• the polymer (Fg) obtainable by the process of the invention typically comprises:
• the pendant side chain of the polymer (Fg) is typically free from fluorine atoms.
• the pendant side chain of the polymer (Fg) is preferably linked to one or two fluorinated backbones of said polymer (Fg) through one or two ester functional groups, said pendant side chain having formula: —[X] y —(CH 2 O) x —(CH 2 CH 2 O) n′ —(CH 2 O) x′ —[X′] y′ — wherein X and X′, equal to or different from each other, are independently bridging groups comprising at least one heteroatom selected from oxygen and nitrogen, x and x′, equal to or different from each other, are independently 0 or 1, y and y′, equal to or different from each other, are independently 0 or 1, and n′ is an integer comprised between 2 and 1000, preferably between 5 and 200.
• the pendant side chain of the polymer (Fg) is more preferably linked to one or two fluorinated backbones of said polymer (Fg) through one or two ester functional groups, said pendant side chain having either of formulae: —CH 2 CH 2 —OC(O)—(CH 2 O)—(CH 2 CH 2 O) n′ — (1) —CH 2 CH 2 O—(CH 2 CH 2 O) n′ — (2) —CH 2 CH 2 O—(CH 2 O)—(CH 2 CH 2 O) n′ — (3) —CH 2 CH 2 O—CH 2 —CH(OH)—(CH 2 O)—(CH 2 CH 2 O) n′ — (4) —CH 2 —CH(OH)—(CH 2 O)—(CH 2 CH 2 O) n′ — (5) —CH 2 CH 2 O—OC(O)NH-E-NHC(O)O—(CH 2 CH 2 O) n′ — (6) wherein in formulae (1) to (6) n′ is an
• the polymer (Fg) preferably comprises, more preferably consists of:
• the polyoxyalkylene is degraded under the process of the invention so that the grafted fluoropolymer thereby provided comprise pendant side chains comprising oxyalkylene recurring units of formula —CH 2 CHR A O— deriving therefrom.
• Determination of the average weight percentage of the oxyalkylene recurring units of formula —CH 2 CHR A O as defined above in the grafted fluoropolymer [polymer (Fg)] of the invention, relative to the total weight of the polymer (Fg), can be performed by any suitable method. Mention can be notably made of NMR techniques, in particular 1 H-NMR techniques, according to standard methods.
• the process of the invention may be further carried out in the presence of at least one polyoxyalkylene (POA) of formula (III): Z—O—(CH 2 CHR A O) n′ —(CH 2 —O) w —H (III) wherein Z is a hydrogen atom or a C 1 -C 5 alkyl group, R A′ is a hydrogen atom or a C 1 -C 5 alkyl group, w is 0 or 1, and n′ is an integer comprised between 2 and 1000, preferably between 5 and 200.
• POA polyoxyalkylene
• polyoxyalkylene (POA) of formula (III) as defined above is typically selected from the group consisting of:
• the polyoxyalkylene (POA) of formula (III) as defined above is preferably a monofunctional POA of formula (III-A) as defined above.
• the weight ratio of the polyoxyalkylene (POA) of formula (I) to the polyoxyalkylene (POA) of formula (III) is typically comprised between 10:90 and 90:10.
• the process is carried out in liquid phase in the presence of one or more organic solvents (S).
• the process is carried out at temperatures typically comprised between 20° C. and 250° C. Temperatures between 20° C. and 150° C., preferably between 20° C. and 80° C. will be preferred.
• Non-limitative examples of suitable organic solvents (S) include, notably, the followings:
• the process is carried out in molten phase at temperatures typically comprised between 100° C. and 300° C., preferably between 150° C. and 250° C., as a function of the melting point of the polymer (F).
• the process is typically carried out with no added organic solvents (S).
• Melt compounders such as extruders, melt kneaders or other devices can be advantageously used to this aim.
• the process of the invention is typically carried out with an equivalent ratio of the polyoxyalkylene (POA) of formula (I) as defined above to the polymer (F) as defined above comprised between 1.0 and 10.0, preferably between 1.0 and 4.0, more preferably between 1.0 and 3.0, even more preferably between 1.0 and 2.0.
• POA polyoxyalkylene
• the hydroxyl groups or the carboxylic acid groups of the polymer (F) as defined above are reacted by polycondensation and/or addition reaction with the reactive groups of the polyoxyalkylene (POA) of formula (I) as defined above thereby providing the grafted fluoropolymer [polymer (Fg)] of the invention comprising oxyalkylene recurring units of formula —CH 2 CHR A O— as defined above.
• the equivalent ratio of the polyoxyalkylene (POA) of formula (I) as defined above to the polymer (F) as defined above is advantageously equal to or higher than 1.0.
• the average molar percentage of the fluorinated backbones of the polymer (F) that reacted with the reactive groups of the polyoxyalkylene (POA) of formula (I) as defined above is typically comprised between 10% and 99% by moles.
• the process comprises reacting:
• This first embodiment of the invention is preferably carried out in liquid phase the presence of at least one organic solvent (S).
• At least one polymer (F) comprising at least one hydroxyl group is contacted with at least one POA of formula (I-A) comprising a reactive group R B comprising at least one sulfonic ester group of formula —OSO 2 R, wherein R is a C 1 -C 8 fluorinated or hydrogenated group optionally comprising one or more aromatic rings, preferably —OSO 2 C 4 F 9 or —OSO 2 —C 6 H 4 —CH 3 , in the presence of at least one organic solvent (S) and at least one catalyst.
• the catalyst is typically selected from organic and inorganic bases.
• the catalyst is preferably an aliphatic tertiary amine, more preferably Et 3 N.
• At least one polymer (F) comprising at least one hydroxyl group is contacted with at least one POA of formula (I-A) comprising a reactive group R B comprising at least one carboxylic acid group, in the presence of at least one organic solvent (S) and at least one catalyst.
• the catalyst is typically selected from organic and inorganic acids, preferably from inorganic acids such as H 2 SO 4 .
• At least one polymer (F) comprising at least one hydroxyl group is contacted with at least one POA of formula (I-A) comprising a reactive group R B comprising at least one isocyanate functional group, in the presence of at least one organic solvent (S) and at least one catalyst.
• the catalyst is typically selected from organic and inorganic bases such as tertiary amines, preferably 1,4-diazabicyclo[2.2.2]octane (DABCO), or Stannous t-butyl laurate.
• organic and inorganic bases such as tertiary amines, preferably 1,4-diazabicyclo[2.2.2]octane (DABCO), or Stannous t-butyl laurate.
• the process comprises reacting:
• This second embodiment of the invention is preferably carried out in molten phase.
• Another object of the present invention is a fluoropolymer film made of a composition (F) comprising at least one polymer (Fg) of the invention.
• composition (F) is advantageously obtained by the process of the invention.
• film By the term “film”, it is hereby intended to denote a dense film having a porosity of less than 5% by volume relative to the total volume of the film.
• the film of the present invention is typically manufactured using techniques commonly known in the art.
• composition (F) is typically processed by coating and drying a fluoropolymer film onto a substrate.
• composition (F) is usually processed by casting, doctor blade coating, metering rod (or Meyer rod) coating, slot die coating, knife over roll coating or “gap” coating, and the like.
• the choice of the substrate is not particularly limited, being understood that the film can be manufactured directly as a unitary assembly or can be manufactured by coating onto another support surface, from which said film can be detached and individualized.
• the fluoropolymer film so obtained may then be post-treated by curing.
• Drying can be performed under modified atmosphere, e.g. under an inert gas, typically exempt notably from moisture (water vapour content of less than 0.001% v/v), or can be performed under vacuum.
• modified atmosphere e.g. under an inert gas, typically exempt notably from moisture (water vapour content of less than 0.001% v/v), or can be performed under vacuum.
• Drying can be performed at room temperature (about 25° C.) or at a temperature exceeding 25° C., this latter condition being generally preferred.
• the drying temperature will be selected so as to effect removal by evaporation of one or more organic solvents (S) from the fluoropolymer film.
• Curing if any, is carried out at temperatures typically comprised between 100° C. and 250° C., preferably between 120° C. and 200° C.
• the low molecular weight side products generated by polycondensation reaction which can be notably water or alcohol, as a function of the nature of the polyoxyalkylene (POA) of formula (I), and one or more organic solvents (S) are at least partially removed from the film, possibly further promoting, by combined action of heat and side products removal, additional polycondensation.
• POA polyoxyalkylene
• S organic solvents
• composition (F) is typically processed in melt-processing techniques.
• composition (F) is usually processed by extrusion through a die at temperatures generally comprised between 100° C. and 300° C., preferably between 100° C. and 250° C., to yield strands which are usually cut for providing pellets.
• Twin screw extruders are preferred devices for accomplishing melt compounding of the composition (F).
• Films can then be manufactured by processing the pellets so obtained through traditional film extrusion techniques.
• the fluoropolymer film so obtained may then be post-treated by curing.
• Curing is carried out at temperatures typically comprised between 100° C. and 250° C., preferably between 120° C. and 200° C.
• the low molecular weight side products generated by polycondensation reaction which can be notably water or alcohol, as a function of the nature of the polyoxyalkylene (POA) of formula (I), are at least partially removed from the fluoropolymer film, possibly further promoting, by combined action of heat and side products removal, additional polycondensation.
• POA polyoxyalkylene
• Another object of the present invention is a porous membrane made of a composition (F) comprising at least one polymer (Fg) of the invention.
• composition (F) is advantageously obtained by the process of the invention.
• porous membrane By the term “porous membrane”, it is hereby intended to denote a membrane having a porosity comprised between 5% and 90%, preferably between 10% and 85% by volume relative to the total volume of the membrane.
• the porous membrane of the invention is typically manufactured by at least one of irradiation, film expansion, template leaching, solution precipitation and electrospinning techniques.
• the porous membrane of the invention is preferably manufactured by the solution precipitation technique.
• a solution comprising the functional fluoropolymer of the invention or compositions thereof is precipitated into two phases, namely a solid, polymer-rich phase which forms the matrix of the membrane and a liquid, polymer-poor phase that forms the membrane pores.
• Polymer precipitation from this solution can be achieved in several ways, such as cooling, solvent evaporation, precipitation by immersion in a non-solvent, imbibition of a non-solvent from the vapour phase.
• the porous membrane of the invention typically has a thickness comprised between 1 ⁇ m and 1000 ⁇ m.
• the membrane of the invention can be under the form of a flat-sheet membrane or can be produced under the form of thin tubes or fibers to yield hollow-fiber membranes.
• Flat-sheet membranes are generally preferred when high fluxes are required.
• Hollow-fiber membranes are particularly preferred when compact modules with high surface areas are required.
• Non-limitative examples of porous membranes which can be obtained using the polymer (Fg) of the invention and compositions (F) thereof include, notably, filtration membranes which can be used in the chemical processing industry in various separation processes, such as micro-filtration and ultra-filtration membranes, in particular porous hollow-fiber membranes for use in water filtration.
• porous membranes so obtained can also be used in biomedical applications, e.g. for haemodialysis, for controlled release of drugs, for artificial organs, such as kidney, lung and pancreas.
• POE-3a HO—(CH 2 CH 2 O)—CH 3 having an average molecular weight of 2000 g/mol.
• POE-3b HO—(CH 2 CH 2 O)—CH 3 having an average molecular weight of 550 g/mol.
• POE-4 C 4 F 9 SO 2 O—(CH 2 CH 2 O)—CH 3 having an average molecular weight of 2282 g/mol.
• the average weight percentage of the oxyalkylene recurring units relative to the total weight of the grafted fluoropolymer was determined by the following equation:
• Porosity of a membrane is a measure of the volume of the pores by the total volume of the membrane.
• the porosities were measured using isopropyl alcohol as wetting fluid according to the procedure notably described in SMOLDERS, K., at al. Terminology for Membrane Distillation. Desalination. 1989, vol. 72, p. 249-262.
• the water permeability was measured with a dead-end stainless steel apparatus applying an atmospheric pressure of 1 bar.
• the surface area of the membranes was about 11 cm 2 .
• the water permeability value is a measure of the hydrophilic properties of the polymer. As the water permeability value increases, the hydrophilic properties of the polymer are increased.
• the contact angle towards water was evaluated at 25° C. by using Dataphysics OCA-20 apparatus, according to ASTM D 5725-99. Measures were taken on flat (dense) surfaces and porous membranes using drops having a volume of 2 ⁇ L.
• the contact angle value towards water is a measure of the hydrophilic properties of the polymer.
• a material is considered hydrophobic when the contact angle of a water droplet on its surface is higher than 90°. As the contact angle towards water decreases, the hydrophilic properties of the polymer are increased.
• Example 2 The same procedure as detailed under Example 1 was followed but setting a temperature of 220° C. and a mixing time of 20 minutes.
• the weight amount of oxyethylene recurring units of formula —CH 2 CH 2 O— was 1.4% by weight, relative to the total weight of the grafted fluoropolymer.
• a grafted fluoropolymer was isolated by precipitating it from NMP with 600 ml of distilled water and washed on a Buchner filtering funnel with an additional 600 ml of distilled water. The functional fluoropolymer was then dried in an oven at 60° C. and 10 mm Hg of residual pressure for 5 hours.
• the weight amount of oxyethylene recurring units of formula —CH 2 CH 2 O— was 1.45% by weight, relative to the total weight of the grafted fluoropolymer.
• Example 3 The same procedure as detailed under Example 3 was followed but using only 60 g of polymer (F-A) having a contact angle towards water of 90°.
• Example 3 The same procedure as detailed under Example 3 was followed but using only 60 g of polymer (F-B) having a contact angle towards water of 90°.
• the coagulation bath consisted of deionized water for Examples 1 to 5 and Comparative Examples 1 and 2.
• the coagulation bath consisted of a 70:30 by weight mixture of deionized water and isopropanol for Examples 6 and 7 and Comparative Example 3. The coagulation bath was kept at 25° C. When the membranes were fully solidified, they were taken out and rinsed in deionized water several times in order to remove the remaining solvent.
• the amount of oxyalkylene recurring units of formula —CH 2 CHR A O— in the grafted fluoropolymers prepared according to Examples 1 to 7 was determined by 1 H-NMR technique as detailed above.
• the weight amount of oxyalkylene recurring units of formula —CH 2 CHR A O— was measured relative to the total weight of the grafted fluoropolymer.
• the water permeability values of the membranes obtained from the grafted fluoropolymers prepared according to Examples 1, 3 and 6 are significantly higher than those of membranes obtained using polymers (F) as such or blends of these polymers (F) with polyoxyalkylenes such as polyoxyethylenes.
• the contact angle value towards water of the grafted fluoropolymer prepared according to Example 4b) is significantly lower than that of polymer (F) as such.

Landscapes

• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Manufacturing & Machinery (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Separation Using Semi-Permeable Membranes (AREA)
• Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
• Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
• Laminated Bodies (AREA)

Applications Claiming Priority (4)

Publications (2)

Family

ID=47561215

Family Applications (1)

Country Status (9)

Families Citing this family (9)

Citations (17)

Family Cites Families (5)

• 2013
  • 2013-12-17 WO PCT/EP2013/076952 patent/WO2014095902A1/en active Application Filing
  • 2013-12-17 EP EP13805926.6A patent/EP2935369B1/en active Active
  • 2013-12-17 KR KR1020157019189A patent/KR102156088B1/ko active IP Right Grant
  • 2013-12-17 HU HUE13805926A patent/HUE034359T2/en unknown
  • 2013-12-17 CA CA2894207A patent/CA2894207C/en active Active
  • 2013-12-17 CN CN201380073620.1A patent/CN105008418B/zh active Active
  • 2013-12-17 AU AU2013361727A patent/AU2013361727B9/en active Active
  • 2013-12-17 JP JP2015548454A patent/JP6377633B2/ja active Active
  • 2013-12-17 US US14/653,406 patent/US9676909B2/en active Active

Patent Citations (17)

Non-Patent Citations (2)

Also Published As

Similar Documents

Legal Events